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(1R,3R)-2-benzyl-6,8-dimethoxy-1,3-dimethyl-1,2,3,4-tetrahydroisoquinoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

178949-48-9

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178949-48-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 178949-48-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,8,9,4 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 178949-48:
(8*1)+(7*7)+(6*8)+(5*9)+(4*4)+(3*9)+(2*4)+(1*8)=209
209 % 10 = 9
So 178949-48-9 is a valid CAS Registry Number.

178949-48-9Relevant academic research and scientific papers

Method and intermediates for the synthesis of korupensamines

-

, (2008/06/13)

Activated isoquinolines and naphthalenes are disclosed which are useful to prepare korupensamines, michellamines and analogs thereof.

The synthesis and biological activity of two analogs of the anti-HIV alkaloid michellamine B

Upender,Pollart,Liu,Hobbs,Olsen,Chao,Bowden,Crase,Thomas,Pandey,Lawson,Dawson

, p. 1371 - 1385 (2007/10/03)

Two simplified analogs of the dimeric naphthalenyltetrahydroisoquinoline alkaloid michellamine B [4',4''-didesmethoxy-2',2''-didesmethylmichellamine B and 6,8-dihydroxy-5-(1',1''-dihydroxy-2',2''-binaphthalen-4'-yl)-1R,3R-dim ethyl-1,2,3,4-tetrahydroisoqu

Biomimetic total synthesis of michellamines A-C

Bringmann, Gerhard,Goetz, Roland,Harmsen, Sven,Holenz, Joerg,Walter, Rainer

, p. 2045 - 2058 (2007/10/03)

The biomimetic first total synthesis of michellamines A, B, and C (1a-c), naturally occurring quateraryl alkaloids with high anti-HIV activity, is described. Key precursors are the molecular "halves" of michellamines, the antimalarial naphthylisoquinoline

Total syntheses of korupensamine C and ancistrobrevine B

Hoye, Thomas R.,Liang, Mi

, p. 3097 - 3098 (2007/10/03)

The first total syntheses of korupensamine C (3) and ancistrobrevine B (4) have been achieved. Important benzyne chemistry related to the construction of the naphthalene moiety, manipulation of methoxy groups on the tetrahydroisoquinoline unit, and hinder

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